I had great plans to write an original piece pulling from recent events and the science. Well this illness had other ideas and kept me awake nearly all night leaving my brain like so much jello.
Then it Hit Me
Plagiarize! Not really but I'm going to provide links to some of the many great efforts made to commemorate the first of what I hope are many bloggerama days.
The Time Is NOW
The ME/CFS community has a great opportunity to help itself like never before and advocates are showing us how. The internet - especially Facebook (yeah XMRV Global Action), forums and Twitter mean we are connected in ways we could never be until recently. Today we are working to fight invalid interpretation and press coverage of scientific studies. Who would have though that possible a couple of years ago? Please do what you can for the cause. It doesn't have to be a blog but please make an effort to help the cause in some small way. We have to be our own advocates.
Here a couple of highlights of but a few of the great blogs put up to commemorate XMRV Bloggerama Day:
Lilly Cooper - An Open Letter To Dr. Elizabeth Unger (link)
Lilly deftly demands the CDC turn it's back on it's sordid history and get it's research focused on bio-medical research rather than the pseudo-scientific course it's pursued for more than two decades beginning with accusations of mass-hysteria. Lilly has turned her talents to blogging lately and is doing a fantastic job.Dr.
Dr. Schweitzer outlines her illness, including her symptoms and many abnormal test results. She points out that her positive XMRV status is but one more abnormal test. The story sounds so familiar. She's lucky to be back on Amligen which helps her function at a greatly-improved level. She points out that an appalling 85% of the ill are undiagnosed and concludes with the words "There are one million people [in the US] with some aspect of my disease, and 850,000 have no diagnosis. Of those who are diagnosed, only a handful are getting treatment. Where are the rest?"
Also, please consider joining the effort called Count Me In - Sick and Disabled Patients Help Raise Awareness of XMRV --- Because Many Lives Depend On It! (link)
The brilliant idea here, as conceived by advocates Maxine Middleton, Vikki Walker, Paul Kayes, Jo Best, is to give a little every month to the WPI to keep research coming. I've pledged to help. Please consider joining.Also a Great Big Thank You to Andrea Pring, the Organizer of Bloggerama Day!
That's all for my feeble little stab at a blog to help push back against those who would use science to harm us rather than help us.
Be Well,
Otis
Here's some background data, mostly for the benefit of Google.
In 2009, Whittemore Peterson Institute scientists discovered a significant link between a newly-found retrovirus, xenotropic murine leukemia virus-related virus (XMRV), and the neuroimmune disease, ME/CFS.
Their ground-breaking discovery was published in the journal Science, on 8th October, 2010.
http://www.wpinstitute.org/xmrv/docs/wpi_pressrel_100809.pdf
http://www.sciencemag.org/content/326/5952/585.abstract?keytype=ref&siteid=sci&ijkey=m3wzKT4yJqEyk
This discovery brought renewed interest to the much-maligned disease and a flurry of research was conducted in order to confirm the link.
On August 23rd 2010, US government scientists validated the link, announcing they had found an association between a family of infectious murine leukaemia viruses and ME/CFS. They reported that 87% of those sampled carried at least one of the retroviruses, along with 7% (1 in 14) of the healthy controls.
http://www.rescindinc.org/fdanihpressconf.mp3
http://www.cfscentral.com/2010/08/fdanihharvard-xmrv-study-same-thing.html
http://www.pnas.org/content/early/2010/08/16/1006901107.full.pdf+html
http://www.pnas.org/content/early/2010/08/16/1007944107.full.pdf+html
XMRV is similar to HIV, the retrovirus that causes AIDS.
Following the validation study several countries banned ME/CFS patients from giving blood. In many cases these bans are for life.
For more information on XMRV and the Whittemore Peterson Institute, please visit the following site: http://www.wpinstitute.org/
____________________
Links and further information.
Key Scientific Papers & Related:
Detection of an Infectious Retrovirus, XMRV, in Blood Cells of Patients with Chronic Fatigue Syndrome Science http://www.sciencemag.org/content/326/5952/585.abstract?keytype=ref&siteid=sci&ijkey=m3wzKT4yJqEyk
Detection of MLV-related virus gene sequences in blood of patients with chronic fatigue syndrome and healthy blood donorshttp://www.pnas.org/content/early/2010/08/16/1006901107.abstract
Aug. 23, 2010 – Detection of MLV-related virus gene sequences in blood of patients with chronic fatigue syndrome and healthy blood donors PNAS FDA Press Briefing http://www.wpinstitute.org/news/docs/FDAbriefing_082310.pdf
Blood Donor Bans:
http://mcwpa.org/in-the-news/blood-donor-bans/
Pertinent News & Blog Reports:
A Big Splash From an Upstart Medical Center New York Times http://www.nytimes.com/2009/11/12/giving/12SICK.html
New Hope in Fatigue Fight Wall Street Journal http://online.wsj.com/article_email/SB10001424052748703846604575447744076968322-lMyQjAxMTAwMDIwMzEyNDMyWj.html
Viruses Found in Chronic Fatigue Syndrome Patients – National Institute of Health NIH Research Matters http://www.nih.gov/researchmatters/august2010/08302010chronicfatigue.htm
The Lingering Mystery of Chronic Fatigue Syndrome http://well.blogs.nytimes.com/2011/01/03/the-lingering-mystery-of-chronic-fatigue-syndrome/?ref=health
Exhausted by Illness, and Doubts http://www.nytimes.com/2011/01/04/health/04fatigue.html
XMRV and CFS – It’s not the end http://www.virology.ws/2010/12/22/xmrv-and-cfs-its-not-the-end/
Gearing Up for the Big Search for XMRV http://blogs.wsj.com/health/2010/11/17/gearing-up-for-the-big-search-for-xmrv/
Other XMRV Links:
Cleveland Clinic – 40% of patients with aggressive prostate cancer have XMRV http://www.plospathogens.org/article/info%3Adoi%2F10.1371%2Fjournal.ppat.0020025
XMRV: Virological, immunological and clinical correlations in patients with chronic lymphocytic leukemia and mantle cell lymphoma http://www.wpinstitute.org/news/docs/Snyderman_XMRV.pdf
Xenotropic Murine Leukemia Virus–related Gammaretrovirus in Respiratory Tract http://www.cdc.gov/eid/content/16/6/1000.htm
COMPOSITIONS AND METHODS RELATING TO XMRV-RELATED DISEASES AND CONDITIONS http://www.wipo.int/pctdb/en/wo.jsp?WO=2010132886&IA=US2010035144&DISPLAY=DESC
Of mice and men: on the origin of XMRV http://www.frontiersin.org/virology/10.3389/fmicb.2010.00147/abstract
XMRV retrovirus found in 62% of ME patients tested in Lillestrøm, Norway
http://esme-eu.com/news/xmrv-retrovirus-found-in-62-of-me-patients-tested-in-lillestroem-norway-article440-7.html
THE PREVALENCE OF XMRV IN HEALTHY BLOOD DONORS IN JAPAN http://www.diagnosesupport.com/health/index.php?option=com_content&view=article&id=305%3Athe-prevalence-of-xenotropic-murine-leukemia-virus-related-virus-in&catid=132%3Axmrv-research&Itemid=8
1st International Workshop on XMRV: Abstracts in Reviews in Antiviral Therapy & Infectious Diseases 2010_8. Abstracts http://regist2.virology-education.com/abstractbook/2010_8.pdf
Distribution of xenotropic murine leukemia virus-related virus (XMRV) infection in chronic fatigue syndrome and prostate cancer Pubmed.gov http://www.ncbi.nlm.nih.gov/pubmed/20842203?dopt=Abstract
A Third Pathogenic and Lymphotropic Human Retrovirus AIDS Review
http://www.aidsreviews.com/files/2010_12_2_121-123.pdf
Great post, Otis, and thanks so much for writing it. Oh, and "Count Me In"!!!! :)
ReplyDeleteWell done. I know jello brain...
ReplyDeletewow - I want some of that jello! Great job Otis.
ReplyDeleteWell done Otis! And thank you for the links to other blogs. I've also joined in donating a small amount to WPI every month, and hope others will do the same where they are able to.
ReplyDeleteThis is such a valuable resource of information! Thank you for the hard work in doing this. I can now point people to this blog and let them read all the great stuff out there. Well done Otis.
ReplyDeleteKeep addding and we will keep reading!!!!! Sarah
Fabulous post, Otis...the time IS now!
ReplyDeleteGreat.
ReplyDeleteWe are all working together.